3-氨基-1-吡咯烷-1-基丙烷-1-酮盐酸盐 | 670253-59-5

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 中文名称: 3-氨基-1-吡咯烷-1-基丙烷-1-酮盐酸盐
• 中文别名: 3-氨基-1-吡咯烷-1-丙烷-1-酮盐酸盐
• 英文名称: [3-oxo-3-(1-pyrrolidinyl)propyl]amine hydrochloride
• 英文别名: 3-amino-1-(pyrrolidin-1-yl)propan-1-one hydrochloride；3-amino-1-pyrrolidin-1-ylpropan-1-one;hydrochloride
• CAS: 670253-59-5
• 化学式: C₇H₁₄N₂O*ClH
• 分子量: 178.662
• InChiKey: CFTPINJPOZAGCI-UHFFFAOYSA-N

物化性质

• 熔点：
  161-164°C

计算性质

• 辛醇/水分配系数(LogP)：
  0.38
• 重原子数：
  11
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.86
• 拓扑面积：
  46.3
• 氢给体数：
  2
• 氢受体数：
  2

安全信息

• 危险等级：
  IRRITANT
• 海关编码：
  2933990090
• 危险性防范说明：
  P233,P260,P261,P264,P271,P280,P302+P352,P304,P304+P340,P305+P351+P338,P312,P321,P332+P313,P337+P313,P340,P362,P403,P403+P233,P405,P501
• 危险性描述：
  H315,H319,H335

反应信息

• 作为反应物：
  描述：

  N-{6-[3-(methylsulfonyl)phenyl]-1,3-benzothiazol-2-yl}-1H-imidazole-1-carboxamide 、 3-氨基-1-吡咯烷-1-基丙烷-1-酮盐酸盐 在 N,N-二异丙基乙胺 作用下， 以 异丁酰胺 为溶剂， 反应 0.42h， 生成 N-{6-[3-(methylsulfonyl)phenyl]-1,3-benzothiazol-2-yl}-N-(3-oxo-3-pyrrolidin-1-ylpropyl)urea
  参考文献：
  名称：

  [EN] FUSED BICYCLIC COMPOUNDS AS INHIBITORS FOR PI3 KINASE
  [FR] COMPOSÉS BICYCLIQUES FUSIONNÉS UTILISÉS COMME INHIBITEURS DE LA PI3 KINASE

  摘要：

  该发明涉及用于调节磷脂酰肌醇3-激酶活性及相关疾病的化合物（I）的公式。

  公开号：

  WO2010100144A1

文献信息

• [EN] BRIDGED SPIRO [2.4] HEPTANE DERIVATIVES AS ALX RECEPTOR AND/OR FPRL2 AGONISTS<br/>[FR] DÉRIVÉS DE SPIRO[2.4]HEPTANE PONTÉS UTILES EN TANT QU'AGONISTES DU RÉCEPTEUR DE ALX ET/OU DU RÉCEPTEUR FPRL2
  申请人：ACTELION PHARMACEUTICALS LTD

  公开号：WO2010134014A1

  公开（公告）日：2010-11-25

  The present invention relates to bridged spiro[2.4]heptane derivatives of formula (I), wherein W, Y, Z, R1 and R2 are as defined in the description, their preparation and their use as pharmaceutically active compounds as ALX receptor and/or FPRL2 agonists for the treatment of inflammatory and obstructive airways diseases.

  本发明涉及桥式螺[2.4]庚烷衍生物的化学式(I)，其中W、Y、Z、R1和R2如描述中所定义，它们的制备及其作为药用活性化合物的ALX受体和/或FPRL2激动剂在治疗炎症性和梗阻性气道疾病中的用途。
• Nitrogen-containing aromatic derivatives
  申请人：Tsuruoka Akihiko

  公开号：US20060004029A1

  公开（公告）日：2006-01-05

  A compound represented by the general formula: wherein X 1 represents a nitrogen atom or a group represented by the formula —CR 10 ═; X 2 represents a nitrogen atom or a group represented by the formula —CR 11 ═; Y represents an oxygen atom or the like; R 1 represents a C 1-6 alkoxy group, an optionally substituted C 6-10 aryloxy group, a group represented by the formula —NR 12a R 12b or the like; R 2 represents a hydrogen atom, an optionally substituted C 1-6 alkyl group, or the like; R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 10 and R 11 each independently represent a hydrogen atom, a halogen atom, an optionally substituted C 1-6 alkyl group, or the like; R 9 represents a group represented by the formula —NR 16a R 16b or the like; and R 12a , R 12b , R 16a and R 16b each independently represent a hydrogen atom, an optionally substituted C 1-6 alkyl group, or the like, a salt thereof, or a hydrate of the foregoing.

  该化合物的通式为：其中X1代表氮原子或代表式为—CR10═的基团；X2代表氮原子或代表式为—CR11═的基团；Y代表氧原子或类似物；R1代表C1-6烷氧基、可选取代的C6-10芳氧基、代表式为—NR12aR12b或类似物的基团；R2代表氢原子、可选取代的C1-6烷基或类似物；R3、R4、R5、R6、R7、R8、R10和R11各自独立地代表氢原子、卤素原子、可选取代的C1-6烷基或类似物；R9代表代表式为—NR16aR16b或类似物的基团；而R12a、R12b、R16a和R16b各自独立地代表氢原子、可选取代的C1-6烷基或类似物，其盐或上述化合物的水合物。
• BRIDGED SPIRO [2.4] HEPTANE DERIVATIVES AS ALX RECEPTOR AND/OR FPRL2 AGONISTS
  申请人：Bur Daniel

  公开号：US20120115841A1

  公开（公告）日：2012-05-10

  The present invention relates to bridged spiro[2.4]heptane derivatives of formula (I), wherein W, Y, Z, R 1 and R 2 are as defined in the description, their preparation and their use as pharmaceutically active compounds as ALX receptor and/or FPRL2 agonists for the treatment of inflammatory and obstructive airways diseases.

  本发明涉及桥联螺[2.4]庚烷衍生物，其化学式为（I），其中W、Y、Z、R1和R2如描述中所定义，其制备以及作为药物活性化合物的ALX受体和/或FPRL2激动剂用于治疗炎症和阻塞性呼吸道疾病。
• C-28 AMINES OF C-3 MODIFIED BETULINIC ACID DERIVATIVES AS HIV MATURATION INHIBITORS
  申请人：Regueiro-Ren Alicia

  公开号：US20130029954A1

  公开（公告）日：2013-01-31

  Compounds having drug and bio-affecting properties, their pharmaceutical compositions and methods of use are set forth. In particular, C-28 amines of C-3 modified betulinic acid derivatives that possess unique antiviral activity are provided as HIV maturation inhibitors. These compounds are useful for the treatment of HIV and AIDS. In particular, the following compounds are provided herein, including pharmaceutically acceptable salts thereof: a compound of formula I a compound of formula II and a compound of formula III

  本文介绍了具有药物和生物影响性质的化合物、它们的制药组合物和使用方法。具体而言，提供了C-3修饰的C-28胺基萜烯酸衍生物，其具有独特的抗病毒活性，可作为HIV成熟抑制剂。这些化合物可用于治疗HIV和艾滋病。特别地，本文提供以下化合物，包括其药学上可接受的盐：I式化合物、II式化合物和III式化合物。
• C-28 amines of C-3 modified betulinic acid derivatives as HIV maturation inhibitors
  申请人：Regueiro-Ren Alicia

  公开号：US08748415B2

  公开（公告）日：2014-06-10

  Compounds having drug and bio-affecting properties, their pharmaceutical compositions and methods of use are set forth. In particular, C-28 amines of C-3 modified betulinic acid derivatives that possess unique antiviral activity are provided as HIV maturation inhibitors. These compounds are useful for the treatment of HIV and AIDS. In particular, the following compounds are provided herein, including pharmaceutically acceptable salts thereof: a compound of formula I a compound of formula II and a compound of formula III

  本发明涉及具有药物和生物影响性质的化合物，以及它们的制药组合物和使用方法。具体而言，提供了具有独特的抗病毒活性的C-3修饰苦杏仁酸衍生物的C-28胺，作为HIV成熟抑制剂。这些化合物可用于治疗HIV和艾滋病。特别地，在此提供以下化合物，包括其药学上可接受的盐：式I的化合物、式II的化合物和式III的化合物。